126330-73-2

Upstream product

• 2127-03-9 2,2'-dipyridyldisulphide 
• 4132-28-9 2,3,4,6-tetra-O-benzyl-D-mannopyranose 
• 100-39-0 benzyl bromide 
• 136984-97-9 2-(β-D-galactopyranosylmercapto)pyridine 
• 2637-34-5 2-Sulfanylpyridine 
• 137037-72-0 2-(2',3',4',6'-tetra-O-acetyl-β-D-galactopyranosylmercapto)pyridine 
• 3068-32-4 1-bromo-1-deoxy-2,3,4,6-tetra-O-acetyl-a-D-galactopyranoside 

Downstream Products

• 117841-66-4 6-O-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-(1->6)-1,2:3,4-di-O-isopropylidene-α-D-galactopyranoside 
• 1430399-00-0 (6-methoxycarbonylpyrid-2-yl)methyl 2,3,4,6-tetra-O-benzyl-α-D-galactopyranoside 
• 41671-29-8 2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl-(1->6)-1,2:3,4-di-O-isopropylidene-α-D-galactopyranose 
• 887700-88-1 1,2-O-isopropylidene-3-O-[6-O-(2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)-2,3,4-tri-O-benzyl-β-D-galactopyranosyl]-1,2-O-sn-glycerol 
• 283177-70-8 C₆₃H₆₈O₁₀S 
• 57731-86-9 3-O-[6-O-(2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)-2,3,4-tri-O-benzyl-β-D-galactopyranosyl]-1,2-O-sn-glycerol 

Relevant academic research and scientific papers

A Glycosylation Protocol Based on Activation of Glycosyl 2-Pyridyl Sulfones with Samarium Triflate

(Equation Presented) Reaction of glycosyl 2-pyridyl sulfones (e.g., 2) with alcohols and samarium(III) triflate affords glycosides in moderate to excellent yields. Benzylated sulfones can be activated in preference to their benzoylated counterparts, and t

Stereoselective synthesis of α-linked saccharides by use of per O-benzylated 2-pyridyl 1-thio hexopyranosides as glycosyl donors and methyl iodide as an activator

A new, practical, stereoselective glycosidation methodology is described where per O-benzylated 2-pyridyl 1-thio-α/β-hexopyranosyl donors of D-gluco-(1), D-galacto- (2), D-manno- (3) and L-rhamno- (4) configurations have been efficiently coupled with dive